Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3756524017 | Occipital pachygyria and polymicrogyria (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3756525016 | Occipital pachygyria and polymicrogyria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3756526015 | Occipital MCD (malformation of cortical development) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3756527012 | A rare genetic cerebral malformation characterized by the presence of cortical smoothening with loss of secondary and tertiary gyri, associated with an excessive number of small, irregular gyri with increased cortical thickness, located in the occipital lobes. Patients usually present with seizures (including myoclonic-astatic, absence, atypical absence, vision loss, myoclonic-atonic, generalized tonic-clonic) and variable (absent to moderate) developmental and/or intellectual delay. There is evidence the disease is caused by homozygous or compound heterozygous mutations in the LAMC3 gene on chromosome 9q34. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3756528019 | A rare genetic cerebral malformation characterised by the presence of cortical smoothening with loss of secondary and tertiary gyri, associated with an excessive number of small, irregular gyri with increased cortical thickness, located in the occipital lobes. Patients usually present with seizures (including myoclonic-astatic, absence, atypical absence, vision loss, myoclonic-atonic, generalised tonic-clonic) and variable (absent to moderate) developmental and/or intellectual delay. There is evidence the disease is caused by homozygous or compound heterozygous mutations in the LAMC3 gene on chromosome 9q34. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4045011000172119 | occipitale pachygyrie en polymicrogyrie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
4045021000172112 | occipitale macrogyrie en polymicrogyrie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Occipital pachygyria and polymicrogyria (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Occipital pachygyria and polymicrogyria (disorder) | Is a | Microgyria | true | Inferred relationship | Some | ||
Occipital pachygyria and polymicrogyria (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Occipital pachygyria and polymicrogyria (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Occipital pachygyria and polymicrogyria (disorder) | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Occipital pachygyria and polymicrogyria (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Occipital pachygyria and polymicrogyria (disorder) | Finding site | Structure of occipital lobe gyrus (body structure) | true | Inferred relationship | Some | 2 | |
Occipital pachygyria and polymicrogyria (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Occipital pachygyria and polymicrogyria (disorder) | Finding site | Structure of occipital lobe gyrus (body structure) | true | Inferred relationship | Some | 1 | |
Occipital pachygyria and polymicrogyria (disorder) | Is a | Macrogyria | true | Inferred relationship | Some | ||
Occipital pachygyria and polymicrogyria (disorder) | Associated morphology | Enlargement (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Occipital pachygyria and polymicrogyria (disorder) | Associated morphology | Congenital smallness | true | Inferred relationship | Some | 1 | |
Occipital pachygyria and polymicrogyria (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets